Gao Xiang Y, Li Lin, Wang Xiao H, Wen Xian Z, Ji Ke, Ye Lin, Cai Jun, Jiang Wen G, Ji Jia F
Beijing Cancer Hospital and Key Laboratory of Carcinogenesis and Translational Research, Department of Gastrointestinal Surgery, Peking University Cancer Hospital and Institute, Beijing 100142, P.R. China.
Cardiff China Medical Research Collaborative, Cardiff University School of Medicine, Heath Park, Cardiff CF14 4XN, UK.
Oncol Rep. 2015 Oct;34(4):1977-87. doi: 10.3892/or.2015.4162. Epub 2015 Jul 30.
Sphingosine-1-phosphate (S1P) plays an important role in regulating many biological processes. Sphingosine-1-phosphate phosphatase 1 (SGPP1) can dephosphorylate S1P into sphingosine and tip the balance of sphingosine-S1P. Increased levels of sphingosine leads to a decrease in the ability of cell invasion as well as an increase in the ability of cell apoptosis. However, little is known regarding the effects of SGPP1 in gastric cancer. The present study examined the function of SGPP1 on gastric cancer cell lines as well as its clinical relevance in gastric cancer progression. Using immunohistochemistry and RT-qPCR techniques, the clinical significance of SGPP1 expression was analyzed in 288 paraffin-embedded gastric tissue specimens and 219 fresh gastric tissues, respectively. Transgenes encoding ribozymes to specifically target human SGPP1 (pEF-SGPP1) was constructed. Human gastric cancer cell lines (AGS and HGC27) were transfected with pEF-SGPP1 transgene and examined by functional analysis. SGPP1 was downregulated in gastric cancer tissues, compared with adjacent normal gastric tissues (p=0.034). SGPP1 mRNA levels in gastric cancer tissues were significantly decreased when compared with their adjacent non-cancerous tissues (p<0.001). Weakly expressed SGPP1 was positively correlated with the lymph node metastasis (p=0.005) and distant metastasis (p=0.031). Kaplan-Meier survival curves revealed that patients with SGPP1 positive expression had a significant increase in overall survival (OS) (p=0.034) and progression-free survival (PFS) (p=0.041). Multivariate analysis indicated the expression of SGPP1 was an independent prognostic factor in gastric cancer patients (p=0.041). In vitro experiments showed that knockdown of SGPP1 resulted in an increase in the invasion (2-fold) and migration (5-fold) of AGS and HGC27. The two gastric cancer cells transfected with pEF-SGPP1 exhibited a slower rate of growth with less adhesion. Thus, our findings provided evidence that SGPP1 may serve as a prognostic biomarker for patients with advanced gastric cancers.
1-磷酸鞘氨醇(S1P)在调节多种生物学过程中发挥着重要作用。1-磷酸鞘氨醇磷酸酶1(SGPP1)可将S1P去磷酸化为鞘氨醇,从而改变鞘氨醇-S1P的平衡。鞘氨醇水平升高会导致细胞侵袭能力下降以及细胞凋亡能力增加。然而,关于SGPP1在胃癌中的作用知之甚少。本研究检测了SGPP1在胃癌细胞系中的功能及其在胃癌进展中的临床相关性。分别使用免疫组织化学和RT-qPCR技术,分析了288例石蜡包埋的胃组织标本和219例新鲜胃组织中SGPP1表达的临床意义。构建了编码特异性靶向人SGPP1的核酶的转基因(pEF-SGPP1)。将pEF-SGPP1转基因转染人胃癌细胞系(AGS和HGC27)并进行功能分析。与相邻正常胃组织相比,胃癌组织中SGPP1表达下调(p=0.034)。与相邻非癌组织相比,胃癌组织中SGPP1 mRNA水平显著降低(p<0.001)。SGPP1低表达与淋巴结转移(p=0.005)和远处转移(p=0.031)呈正相关。Kaplan-Meier生存曲线显示,SGPP1阳性表达的患者总生存期(OS)(p=0.034)和无进展生存期(PFS)(p=0.041)显著增加。多变量分析表明,SGPP1的表达是胃癌患者的独立预后因素(p=0.041)。体外实验表明,敲低SGPP1会导致AGS和HGC27的侵袭能力(2倍)和迁移能力(5倍)增加。转染pEF-SGPP1的两种胃癌细胞生长速度较慢,黏附性较低。因此,我们的研究结果提供了证据表明SGPP1可能作为晚期胃癌患者的预后生物标志物。